Evidence map›Paper›PMID 30586871›Full record

ReviewPharmaceutics2018

Engineering of Nanofibrous Amorphous and Crystalline Solid Dispersions for Oral Drug Delivery.

Laura Modica de Mohac, Alison Veronica Keating, Maria de Fátima Pina, Bahijja Tolulope Raimi-Abraham

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Laura Modica de MohacDIBIMIS Department, University of Study of Palermo, 90128 Palermo, Italy. laura.modicademohac@unipa.it.ORCID 0000-0002-4515-1342
Alison Veronica KeatingDrug Delivery Group, Institute of Pharmaceutical Science Faculty of Life Sciences and Medicine, King's College London, London SE1 9NH, UK. Alison.Keating@kcl.ac.uk.
Maria de Fátima PinaDepartment of Pharmaceutics, University College London School of Pharmacy, London WC1N 1AX, UK. mariafatima.gpina@gmail.com.
Bahijja Tolulope Raimi-AbrahamDrug Delivery Group, Institute of Pharmaceutical Science Faculty of Life Sciences and Medicine, King's College London, London SE1 9NH, UK. bahijja.raimi-abraham@kcl.ac.uk.ORCID 0000-0002-5330-3967

Funding

Erasmus plus programme 00000000
6 · The paper itself

Abstract

Poor aqueous solubility (<0.1 mg/mL) affects a significant number of drugs currently on the market or under development. Several formulation strategies including salt formation, particle size reduction, and solid dispersion approaches have been employed with varied success. In this review, we focus primarily on the emerging trends in the generation of amorphous and micro/nano-crystalline solid dispersions using electrospinning to improve the dissolution rate and in turn the bioavailability of poorly water-soluble drugs. Electrospinning is a simple but versatile process that utilizes electrostatic forces to generate polymeric fibers and has been used for over 100 years to generate synthetic fibers. We discuss the various electrospinning studies and spinneret types that have been used to generate amorphous and crystalline solid dispersions.

Indexed as

amorphousaqueous solubility enhancementcrystallineelectrospinningoral drug deliverysolid dispersion

Identifiers

PMID30586871
PMCPMC6359107

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.